Placebo-level incidence of extrapyramidal symptoms (EPS) with quetiapine in controlled studies of patients with bipolar mania

Bipolar Disord. 2006 Oct;8(5 Pt 1):467-74. doi: 10.1111/j.1399-5618.2006.00350.x.

Abstract

Objectives: To evaluate extrapyramidal symptoms (EPS), including akathisia, with quetiapine in patients with bipolar mania.

Methods: Data were analyzed from four similarly designed, randomized, double-blind, 3- to 12-week studies. Two studies evaluated quetiapine monotherapy (up to 800 mg/day) (n = 209) versus placebo (n = 198), with lithium or haloperidol monotherapy as respective active controls. Two studies evaluated quetiapine (up to 800 mg/day) in combination with a mood stabilizer (lithium or divalproex, QTP + Li/DVP) (n = 196) compared to placebo and mood stabilizer (PBO + Li/DVP) (n = 203). Extrapyramidal symptoms were evaluated using the Simpson-Angus Scale (SAS), the Barnes Akathisia Rating Scale (BARS), adverse event reports and anticholinergic drug usage.

Results: The incidence of EPS-related adverse events, including akathisia, was no different with quetiapine monotherapy (12.9%) than with placebo (13.1%). Similarly, EPS-related adverse events with QTP + Li/DVP (21.4%) were no different than with PBO + Li/DVP (19.2%). Adverse events related to EPS occurred in 59.6% of patients treated with haloperidol (n = 99) monotherapy, whereas 26.5% of patients treated with lithium (n = 98) monotherapy experienced adverse events related to EPS. The incidence of akathisia was low and similar with quetiapine monotherapy (3.3%) and placebo (6.1%), and with QTP + Li/DVP (3.6%) and PBO + Li/DVP (4.9%). Lithium was associated with a significantly higher incidence (p < 0.05) of tremor (18.4%) than quetiapine (5.6%); cerebellar tremor, which is a known adverse effect of lithium, may have contributed to the elevated rate of tremor in patients receiving lithium therapy. Haloperidol induced a significantly higher incidence (p < 0.001) of akathisia (33.3% versus 5.9%), tremor (30.3% versus 7.8%), and extrapyramidal syndrome (35.4% versus 5.9%) than quetiapine. No significant differences were observed between quetiapine and placebo on SAS and BARS scores. Anticholinergic use was low and similar with quetiapine or placebo.

Conclusions: In bipolar mania, the incidence of EPS, including akathisia, with quetiapine therapy is similar to that with placebo.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Akathisia, Drug-Induced / diagnosis*
  • Akathisia, Drug-Induced / psychology
  • Anticonvulsants / adverse effects
  • Anticonvulsants / therapeutic use
  • Antimanic Agents / adverse effects
  • Antimanic Agents / therapeutic use
  • Antipsychotic Agents / adverse effects*
  • Antipsychotic Agents / therapeutic use
  • Basal Ganglia Diseases / chemically induced*
  • Basal Ganglia Diseases / diagnosis
  • Basal Ganglia Diseases / psychology
  • Bipolar Disorder / diagnosis
  • Bipolar Disorder / drug therapy*
  • Bipolar Disorder / psychology
  • Dibenzothiazepines / adverse effects*
  • Dibenzothiazepines / therapeutic use
  • Double-Blind Method
  • Drug Therapy, Combination
  • Female
  • Haloperidol / adverse effects
  • Haloperidol / therapeutic use
  • Humans
  • Lithium Compounds / adverse effects
  • Lithium Compounds / therapeutic use
  • Male
  • Middle Aged
  • Multicenter Studies as Topic
  • Neurologic Examination / drug effects
  • Quetiapine Fumarate
  • Randomized Controlled Trials as Topic / standards*
  • Risk
  • Treatment Outcome
  • Valproic Acid / adverse effects
  • Valproic Acid / therapeutic use

Substances

  • Anticonvulsants
  • Antimanic Agents
  • Antipsychotic Agents
  • Dibenzothiazepines
  • Lithium Compounds
  • Quetiapine Fumarate
  • Valproic Acid
  • Haloperidol